C₁₅H₂₁N₃O₂S₂

Base Information

Chemical Name:C₁₅H₂₁N₃O₂S₂
CAS No.:1346644-95-8
Molecular Formula:C₁₅H₂₁N₃O₂S₂
Molecular Weight:339.483
Hs Code.:

C<sub>15</sub>H<sub>21</sub>N<sub>3</sub>O<sub>2</sub>S<sub>2</sub>

Synonyms:C₁₅H₂₁N₃O₂S₂

Suppliers and Price of C₁₅H₂₁N₃O₂S₂

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₁₅H₂₁N₃O₂S₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₅H₂₁N₃O₂S₂

There total 6 articles about C₁₅H₂₁N₃O₂S₂ which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 266993-72-0
3-carbamoylbenzene-1,2-diaminium dichloride

: 1077-28-7,62-46-4
Thioctic acid

: 1346644-95-8
C₁₅H₂₁N₃O₂S₂

Guidance literature:: Thioctic acid; With pyridine; 1,1'-carbonyldiimidazole; In N,N-dimethyl-formamide; at 45 ℃; for 0.5h;

3-carbamoylbenzene-1,2-diaminium dichloride; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 641-70-3
3-nitrophthalic acid anhydride

: 1346644-95-8
C₁₅H₂₁N₃O₂S₂

Guidance literature:: Multi-step reaction with 5 steps

1.1: ammonium hydroxide

2.1: potassium hydroxide; bromine / Heating

3.1: thionyl chloride

4.1: Raney nickel / ethyl acetate; ethanol

5.1: pyridine; 1,1'-carbonyldiimidazole / N,N-dimethyl-formamide / 0.5 h / 45 °C

5.2: 20 °C

With pyridine; ammonium hydroxide; thionyl chloride; bromine; 1,1'-carbonyldiimidazole; potassium hydroxide; Raney nickel; In ethanol; ethyl acetate; N,N-dimethyl-formamide; 2.1: Hofmann Rearrangement;

Reference yield:

: 313279-12-8
2-amino-3-nitro-benzamide

: 1346644-95-8
C₁₅H₂₁N₃O₂S₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: Raney nickel / ethyl acetate; ethanol

2.1: pyridine; 1,1'-carbonyldiimidazole / N,N-dimethyl-formamide / 0.5 h / 45 °C

2.2: 20 °C

With pyridine; 1,1'-carbonyldiimidazole; Raney nickel; In ethanol; ethyl acetate; N,N-dimethyl-formamide;